Canonical Allele Identifier: CA406502864

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46919000C>T , CM000681.2:g.46919000C>T	GRCh38
NC_000019.9:g.47422257C>T , CM000681.1:g.47422257C>T	GRCh37
NC_000019.8:g.52114097C>T	NCBI36
NG_047014.1:g.5434C>T
NG_047014.2:g.63004C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004491.5:c.325C>T MANE Select	NP_004482.4:p.Arg109Ter
ENST00000672722.1:c.325C>T MANE Select	ENSP00000500409.1:p.Arg109Ter
NM_004491.4:c.325C>T	NP_004482.4:p.Arg109Ter
ENST00000404338.7:c.325C>T	ENSP00000385720.2:p.Arg109Ter
ENST00000404338.8:c.325C>T	ENSP00000385720.2:p.Arg109Ter
ENST00000614079.1:c.325C>T	ENSP00000483730.1:p.Arg109Ter
ENST00000615647.1:c.325C>T	ENSP00000479487.1:p.Arg109Ter
XM_011526873.1:c.325C>T	XP_011525175.1:p.Arg109Ter
XM_024451473.1:c.325C>T	XP_024307241.1:p.Arg109Ter
XR_002958305.1:n.434C>T
XR_935811.1:n.434C>T